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Up to: Syndromic disease · Neurodevelopmental disorder · Partial deletion of the long arm of chromosome 7
Williams syndrome
A rare genetic multisystemic neurodevelopmental disorder characterized by a distinct facial appearance, cardiac anomalies (most frequently supravalvular aortic stenosis), cognitive and developmental abnormalities, and connective tissue abnormalities (such as joint laxity)
This condition has no sub-types.